Canonical Allele Identifier: CA2026352308
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32878933T= , CM000674.2:g.32878933T= GRCh38
NC_000012.11:g.33031867T= , CM000674.1:g.33031867T= GRCh37
NC_000012.10:g.32923134T= NCBI36
NG_009000.1:g.22914A= , LRG_398:g.22914A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700559.2:c.323A= ENSP00000515065.2:p.Tyr108=
ENST00000700563.2:c.323A= ENSP00000515066.2:p.Tyr108=
ENST00000700563.1:c.277A=
ENST00000700564.1:n.327A=
ENST00000700565.1:n.176A=
ENST00000070846.11:c.323A= ENSP00000070846.6:p.Tyr108=
ENST00000340811.9:c.323A= MANE Select ENSP00000342800.5:p.Tyr108=
ENST00000070846.10:c.323A= ENSP00000070846.6:p.Tyr108=
ENST00000340811.8:c.323A= ENSP00000342800.4:p.Tyr108=
ENST00000613243.1:c.323A= ENSP00000478295.1:p.Tyr108=
NM_001005242.2:c.323A= NP_001005242.2:p.Tyr108=
NM_004572.3:c.323A= , LRG_398t1:c.323A= NP_004563.2:p.Tyr108=
NM_001005242.3:c.323A= MANE Select NP_001005242.2:p.Tyr108=
NM_004572.4:c.323A= NP_004563.2:p.Tyr108=